Near-infrared afterglow semiconducting nano-polycomplexes for multiplex differentiation of cancer exosomes
The detection of exosomes is promising for the early diagnosis of cancer. However, the development of suitable optical sensors remains challenging. We have developed the first luminescent nanosensor for the multiplex differentiation of cancer exosomes that bypasses real‐time light excitation. The se...
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sg-ntu-dr.10356-826152023-02-28T17:07:22Z Near-infrared afterglow semiconducting nano-polycomplexes for multiplex differentiation of cancer exosomes Lyu, Yan Cui, Dong Huang, Jiaguo Fan, Wenxuan Miao, Yansong Pu, Kanyi School of Chemical and Biomedical Engineering School of Biological Sciences Exosomes Biosensors Engineering::Chemical engineering The detection of exosomes is promising for the early diagnosis of cancer. However, the development of suitable optical sensors remains challenging. We have developed the first luminescent nanosensor for the multiplex differentiation of cancer exosomes that bypasses real‐time light excitation. The sensor is composed of a near‐infrared semiconducting polyelectrolyte (ASPN) that forms a complex with a quencher‐tagged aptamer. The afterglow signal of the nanocomplex (ASPNC), being initially quenched, is turned on in the presence of aptamer‐targeted exosomes. Because detection of the afterglow takes place after the excitation, background signals are minimized, leading to an improved limit of detection that is nearly two orders of magnitude lower than that of fluorescence detection in cell culture media. Also, ASPNC can be easily tailored to detect different exosomal proteins by changing the aptamer sequence. This enables an orthogonal analysis of multiple exosome samples, potentially permitting an accurate identification of the cellular origin of exosomes for cancer diagnosis. MOE (Min. of Education, S’pore) Accepted version 2019-07-18T02:49:32Z 2019-12-06T14:59:02Z 2019-07-18T02:49:32Z 2019-12-06T14:59:02Z 2019 2019 Journal Article Lyu, Y., Cui, D., Huang, J., Fan, W., Miao, Y., & Pu, K. (2019). Near-infrared afterglow semiconducting nano-polycomplexes for the multiplex differentiation of cancer exosomes. Angewandte Chemie International Edition, 58(15), 4983-4987. doi:10.1002/anie.201900092 1433-7851 https://hdl.handle.net/10356/82615 http://hdl.handle.net/10220/49417 10.1002/anie.201900092 213962 en Angewandte Chemie International Edition This is the peer reviewed version of the following article: Lyu, Y., Cui, D., Huang, J., Fan, W., Miao, Y., & Pu, K. (2019). Near-infrared afterglow semiconducting nano-polycomplexes for the multiplex differentiation of cancer exosomes. Angewandte Chemie International Edition, 58(15), 4983-4987. doi:10.1002/anie.201900092, which has been published in final form at https://dx.doi.org/10.1002/anie.201900092. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. 5 p. application/pdf |
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Exosomes Biosensors Engineering::Chemical engineering Lyu, Yan Cui, Dong Huang, Jiaguo Fan, Wenxuan Miao, Yansong Pu, Kanyi Near-infrared afterglow semiconducting nano-polycomplexes for multiplex differentiation of cancer exosomes |
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The detection of exosomes is promising for the early diagnosis of cancer. However, the development of suitable optical sensors remains challenging. We have developed the first luminescent nanosensor for the multiplex differentiation of cancer exosomes that bypasses real‐time light excitation. The sensor is composed of a near‐infrared semiconducting polyelectrolyte (ASPN) that forms a complex with a quencher‐tagged aptamer. The afterglow signal of the nanocomplex (ASPNC), being initially quenched, is turned on in the presence of aptamer‐targeted exosomes. Because detection of the afterglow takes place after the excitation, background signals are minimized, leading to an improved limit of detection that is nearly two orders of magnitude lower than that of fluorescence detection in cell culture media. Also, ASPNC can be easily tailored to detect different exosomal proteins by changing the aptamer sequence. This enables an orthogonal analysis of multiple exosome samples, potentially permitting an accurate identification of the cellular origin of exosomes for cancer diagnosis. |
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School of Chemical and Biomedical Engineering |
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School of Chemical and Biomedical Engineering Lyu, Yan Cui, Dong Huang, Jiaguo Fan, Wenxuan Miao, Yansong Pu, Kanyi |
format |
Article |
author |
Lyu, Yan Cui, Dong Huang, Jiaguo Fan, Wenxuan Miao, Yansong Pu, Kanyi |
author_sort |
Lyu, Yan |
title |
Near-infrared afterglow semiconducting nano-polycomplexes for multiplex differentiation of cancer exosomes |
title_short |
Near-infrared afterglow semiconducting nano-polycomplexes for multiplex differentiation of cancer exosomes |
title_full |
Near-infrared afterglow semiconducting nano-polycomplexes for multiplex differentiation of cancer exosomes |
title_fullStr |
Near-infrared afterglow semiconducting nano-polycomplexes for multiplex differentiation of cancer exosomes |
title_full_unstemmed |
Near-infrared afterglow semiconducting nano-polycomplexes for multiplex differentiation of cancer exosomes |
title_sort |
near-infrared afterglow semiconducting nano-polycomplexes for multiplex differentiation of cancer exosomes |
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2019 |
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https://hdl.handle.net/10356/82615 http://hdl.handle.net/10220/49417 |
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